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Randomized controlled study on the treatment of post-stroke spasticity by massage based on Tiaozang Shujing theory and acupuncture

Randomized controlled study on the treatment of post-stroke spasticity by massage based on Tiaozang Shujing theory and acupuncture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088304
Enrollment
Unknown
Registered
2024-08-15
Start date
2024-08-15
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-stroke spasticity

Interventions

Experimental group:Tiaozang Shujing massage +acupuncture
control group:Conventional massage treatment +acupuncture

Sponsors

The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnostic criteria for stroke and supported by imaging data such as cranial CT or MRI; 2. Age between 18 and 75 years old, gender not limited; 3. The patient is conscious, with vital signs lying flat and normal cognitive ability. The course of the disease is within 6 months; 4. The Brunstrom staging of the affected limb is in stages II-IV, and the modified Ashworth assessment is in grades 1-3, accompanied by symptoms of increased muscle tone in the paralyzed affected limb; 5. Those who have not taken any Chinese or Western sedatives or muscle relaxants within two weeks; 6. Those who voluntarily participate in this clinical trial, comply with the diagnosis and treatment plan, and sign the informed consent form. ? Note: To be included, the above six items must be met simultaneously.

Exclusion criteria

Exclusion criteria: 1. Those who have had at least 3 strokes; 2. Confirmed through examination that limb spasms are caused by other diseases; 3. Those who have received other treatments; 4. Merge patients with severe underlying diseases and mental illnesses; 5. Patients with subarachnoid hemorrhage, other bleeding disorders or coagulation dysfunction; 6. Pregnant or lactating women. ? Note: Any of the above conditions shall be excluded from this study.

Design outcomes

Primary

MeasureTime frame
Modified Ashworth Scale;Barthel Index;simplified Fugl-Meyer Assessment;

Secondary

MeasureTime frame
EMG integral value detection;

Countries

China

Contacts

Public ContactJiang Tao

The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine

13956082716@163.com+86 139 5608 2716

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026